Research and development technician jobs in Southaven, MS - 30 jobs

Category Laboratory Sciences & Support Department Hematology Shift Weekday Day Type Full Time Scheduled Weekly Hours 40 Req # JR6075 Job Description The Scientist performs and/or coordinates a wide range of laboratory research procedures and conducts a spectrum of complex support tasks and projects determined by the field and scope of the particular research study. Also, performs a variety of laboratory techniques independently and presents results. The Associate Scientist performs a variety of moderately complex research tasks determined by the field and scope of the particular research project/study. Also, performs tasks related to the research project independently, but within broad guidelines and subject to periodic review by supervisor or other research staff. At St. Jude Children's Research Hospital, talented faculty and staff work together and with colleagues worldwide to advance the research and treatment of pediatric cancer and other catastrophic diseases. We are seeking an outstanding, highly motivated, and creative Scientist to join Dr. Jonathan Yen's lab and the Therapeutic Genome Engineering (TGEn) group. You will be part of a multidisciplinary team of scientists and clinical researchers helping to advance genome editing strategies for treating sickle cell disease to a Phase 1 clinical trial. Our ongoing therapeutic pipeline is fueled by internal scientific discoveries directed from "bench-to-bedside" and academic collaborations. Come join TGEn to en GENEer concepts to cures! You will have the opportunity to work with a talented interdisciplinary team of scientists to develop a cellular therapy with the goal of treating patients here at St. Jude Children's Research Hospital and worldwide. The ideal candidate will have a strong combination of experience with genome editing and human hematopoietic stem cells (HSCs). You will also have the opportunity to learn about and support new, exciting projects, including the development and optimization of pre-clinical genome editing strategies to treat hemoglobinopathies and other hematological diseases, process development, and IND-enabling studies (Pharm/Tox). Job Responsibilities: * Perform studies to develop genome editing strategies for human hematopoietic stem cells (HSC). * Design and execute IND-enabling experiments to characterize the pharmacology of a genome-edited human hematopoietic stem cell product to treat sickle cell disease. * Characterize the efficacy, safety, and potency of the HSC cellular drug product in in vitro and xenotransplantation assays. * Multicolor flow cytometry and FACS to sort hematopoietic populations of relevance. * Develop experimental methods including RT-PCR, dd PCR, next-generation sequencing, and single-cell sequencing. * Perform NGS library preparation and analysis of editing outcomes, on-target and off-target. * Evaluate scale-up and close-system processes to ensure reproducibility of the drug product. * Conduct exploratory research on developing novel in-vitro and in-vivo delivery strategies. * Interact and collaborate with multidisciplinary teams to advance the program. * Establish tracking and trending analyses of process development and pilot runs. * Draft documentation (protocols, batch records, reports) to standardize and transfer process to GMP facility. * Maintains regular and predictable attendance. * Performs other related duties as assigned to meet the goals of the department and institution. Minimum Education and/or Training: * Bachelor's degree in a relevant scientific area is required. * Master's or PhD degree in a relevant scientific area is highly preferred. Associate Scientist Minimum Experience: * 7 + years of research experience is required * 5 + years of research experience is required with a Master's degree * 2 + years of research experience is required with a PHD * Experience leading and supporting research experiments preferred * Some experience leading lab and scientific project coordination, maintenance, and other research support activities preferred * Experience in guiding and training other laboratory personnel preferred * Proven performance in earlier role/comparable role Salary range: $65,520.00 - $114,400.00 Scientist Minimum Experience: * Eight (8) years of relevant post-degree work experience is required with a Bachelor's degree. * Six (6) years of relevant post-degree work experience is required with a Master's degree. * Three (3) years of relevant post-degree work experience is required with a PhD. * Experience leading and supporting research experiments preferred. * Some experience leading lab and scientific project coordination, maintenance, and other research support activities preferred. * Experience in guiding and training other laboratory personnel preferred. * Proven performance in earlier role/comparable role. Salary range: $86,320.00 - $154,960.00 Welcome to Memphis This position is based in Memphis, TN; relocation assistance is available. Memphis is a family-friendly metropolitan area that more than a million residents call home. Memphis is recognized for its world-class music, food, and hospitality. Cost of living is one of our biggest attractions; in fact, Money listed Memphis as one of the least expensive cities in which to raise a child. Mild winters and beautiful green spaces make the city a magnet for outdoor enthusiasts - there are over 200 miles of bike-friendly lanes with more being added. Forbes recently named Memphis the 4th happiest city in which to work. Apply today! A cover letter is highly recommended. Interested applicants should submit a cover letter as part of the application process. Please address your cover letter to: Jonathan Yen, PhD Department of Hematology Mail Stop 355 St. Jude Children's Research Hospital 262 Danny Thomas Place Memphis, TN 38105-3678 Compensation In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $86,320 - $154,960 per year for the role of Associate Scientist or Scientist - Yen Lab/Therapeutic Genome Engineering (TGEn Group). Explore our exceptional benefits! St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. This position is responsible for working in a cross-functional team of scientists and engineers to deliver on milestones associated with the entire lifecycle of additive-manufactured (AM), orthopedic products (i.e., early-phase research, new product development and product support). The individual is expected to apply his or her knowledge and practical skills in the field of materials science and engineering and additive manufacturing to serve as a technical leader within project teams and manage large-scope projects. With a minimal level of guidance, the individual will develop and execute testing plans, evaluate testing risk, and ensure adherence to all appropriate standards and documentation requirements. The individual's decisions will be guided by the existing policies, procedures, and business plans. What will you be doing? * Design and conduct AM research studies to support the business throughout the product lifecycle. Work with minimal guidance and within cross-functional teams to achieve milestones for research programs where key focus is additive manufacturing, materials research, and materials process development. Work in a cross-functional team and provide direction on materials testing (internal vs external) based on capacity and capability. Liaise with regulatory bodies for testing requirements. Comply with laboratory management system according to international (e.g., ISO 17025) and S&N standards. * Write, present and review test reports, retrieval reports, research manuscripts, presentations, white papers, customer communication documents, and invention disclosures related to materials research, process development and AM. Liaise with the national as well as international regulatory bodies as needed. Use expertise to solve unique and complex problems with broad impact on the business using innovative solutions. Propose, initiate, co-ordinate and review appropriate internal or external studies that will satisfy internal and external testing requirements. Communicate test plans and results to senior management as needed. Interact with and present to internal or external experts, HCPs, etc. * Maintain strong knowledge of the AM and Ortho industries, current technical developments, customer needs and business opportunities to match unmet needs with AM solutions. Prepare presentations and technical material needed for sales, marketing and medical education teams as needed. * Comply with the laboratory management practices set-up by the management including S&N global health, safety and environment practices. Create work instructions for safe and effective use of equipment in the laboratory. Manage laboratory equipment maintenance and calibration with internal and external resources. Assist other members of the team to order laboratory consumables, assist in the management of budgets and write capital requests as needed. * Perform administrative functions as necessary (objective setting, development plans, training, self-appraisal, etc.). Write technical reports and ensure maintenance of complete and accurate records for all controlled documentation. Other miscellaneous activities include attending meetings, submitting financial/travel requests, coordinating team activities, conducting tours and making presentations. What will you need to be successful? * In-depth knowledge of metal additive-manufacturing methods like laser powder bed fusion, e-beam powder bed fusion and/or binder jetting * In-depth knowledge of the relationship between materials processing, microstructure and properties * Experience characterizing materials via various methods (e.g., mechanical testing, metallography, microscopy, etc.) * Bachelor of Science, Master of Science or Ph.D. in Mechanical, Materials, or Biomedical Engineering, or another appropriate field. * Must have good team and communication skills. Requires use of email, internet and Microsoft Office software. * 0 - 4 years hands-on experience. * While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; and talk or hear. The employee frequently is required to walk. The employee is occasionally required to sit and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, depth perception, and the ability to adjust focus. You Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve. * Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website ( ******************************* * Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement * Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day * Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program * Flexibility: Hybrid Work Model (For most professional roles) * Training: Hands-On, Team-Customized, Mentorship * Extra Perks: Discounts on fitness clubs, travel and more! #LI-HYBRID Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability. Stay connected by joining our Talent Community. We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day. Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description They must have protein purification experience including non-labeled proteins and They are NOT looking for candidates with molecular/PCR/gene cloning, etc. Summary Description: Position will be responsible for overseeing and executing the process design and manufacturing of monoclonal antibodies, polyclonal antibodies and recombinant proteins products and services sold into IVD industry. The Senior Manufacturing Process Scientist will possess ‘hands-on' experience with various forms of chromatography (affinity, ion exchange, HIC, etc.), centrifugation, TFF/DF/UF, cell culture and fermentation. Experience with aseptic techniques particularly useful in the areas of eukaryotic cell culture, bacterial and yeast fermentation. The individual must be capable of executing and authoring Master Batch Records and Standard Operating Procedures in compliance with current Good Manufacturing Practices. This position will supervise Production Technicians. Duties: o Perform bio separation of recombinant proteins, monoclonal/polyclonal antibodies. Bioseparation methods to include, but not limited to, preparative centrifugation, TFF filtration, and chromatographic methods (ion exchange, size exclusion, affinity, etc.). o Familiar with In vitro cell culture of monoclonal antibodies and fermentation of recombinant proteins. o Develop and perform various analytical protein methods for process monitoring and characterization of in-process and final product. The methods to include but not limited to SDS-PAGE, Western Blot, ELISA, UV-VIS, and Immunoassays methods. o Assess feasibility of contract manufacturing cell culture and purification opportunities, participate in development of proposal and costing estimates. o Author master batch records and SOPs for transferred/developed process in compliance with all current GMP regulations and company SOPs. o Train Production Technicians in upstream and downstream manufacturing processes. o Develop strategies to improving yields and reducing overall manufacturing costs. Investigate alternative materials or new process equipment to improve efficiency. o Write and execute validation protocols for new and existing manufacturing processes. o Assist with the writing of technical reports, customer proposals, and product release specifications Qualifications Required Qualifications: o Ph.D. with 3+ years of industrial experience or MS with 6+ years of industrial experience in a GMP or GLP environment. o Extensive knowledge and hands on experience of protein purification and characterization. o Experience with virus like proteins and viruses a plus. A knowledge of AKTA Unicorn software and disposable systems a plus. o Hands on experience with in vitro cell culture and recombinant protein fermentation o Ability to independently apply bioseparation basic theory and scientific principles to conduct downstream process development for proteins. o Proven experience with process scale-up procedures. o Extensive knowledge and hands on experience with protein analytical methods including (SDS-PAGE, Western Blot, ELISA, BCA, UV-VIS, HPLC methods etc). o Concise and accurate oral and written reporting of technical including batch records, SOPs, validation protocols and customer proposals. Requirements (Physical, Mental, Environmental Demands): o Ability to walk up and down several flights of stairs throughout the work day in a multi-location facility. o Must be able to concentrate, analyze and solve complex issues throughout the course of the work day. o Ability to work on a PC including repetitive use of a keyboard and mouse for long periods throughout the course of the work day. o Ability to sit for long periods of time, stoop, reach, bend throughout the course of the work day. o Must be able to lift up to 30lbs. multiple times daily. o Must be able to travel by air/car to other locations of MBI as needed. o May be required to work outside normal business hours including evenings and/or weekends to support business needs. Additional Information Manisha Jathar 732 429 1850

WHO WE ARE Helena Agri-Enterprises, LLC is a leading full-service agronomic solutions provider that's been in business since 1957. Our first location was in West Helena, Arkansas hence the name "Helena". We now have 450+ locations nationwide and over 6,000 employees. Our corporate office is located in Collierville, Tennessee, a suburb outside of Memphis. Year after year we rank at the top nationally for volume and sales in our industry. There are many facets to our company including product development, sales, operations, precision technology and manufacturing just to name a few. ABOUT THE JOB The Technical Solutions Chemist is a valuable member of the Helena Products Group (HPG) team. This position is responsible for performing a wide range of tests and investigation services required to support the HPG portfolio, which includes adjuvant, bioscience, fertilizer and crop protection products. This individual will fill an important need for the organization by providing field-facing technical support services for these products. This position is with Helena Products Group (HPG). HPG develops Helena's extensive portfolio of proprietary products that includes seven product categories covering both crop production and crop protection. HPG leads the industry in creating innovations and formulation technologies and operates out of a state-of-the-art research, development and training facility located in Memphis, TN. WHAT YOUR DAY WILL LOOK LIKE Bench tests physical properties of agriculture products, such as pH, density, contact angle, water content, surface tension, viscosity, emulsion performances and flashpoint. Assists in screening pure and diluted product mixtures for compatibility and reports findings. Helps troubleshoot mixing and quality complaints submitted by Helena field team members and other end users. Tests samples involved in Product Quality Notifications and competitive product analysis. Performs testing needed for technical bulletins, product support bulletins and additional training documents. Performs qualitative tests on HPG and competing products for development of new product demonstrations. Participates in lab tours for employee and customer groups. Aids in development and implementation of new laboratory methods and protocols. Collects data and keeps appropriate records on all testing. Reports results to leader in a timely manner. Maintains physical and electronic document storage including Safety Data Sheets. Maintains chemical inventory, instruments, equipment, glassware and laboratory spaces. Cleans glassware per Standard Operating Procedures (SOP) instructions. May be required to operate a company vehicle. Provides excellent customer service to all internal and external customers. Other work-related duties as assigned by leader. Reliable and regular attendance is required. Follows all company policies and procedures. EDUCATION & EXPERIENCE Bachelor of Science degree in chemistry, biology, agriculture or related field is required. or a high school diploma and five years of experience in chemistry or related field is required. One year of laboratory experience is required. SKILLS & QUALIFICATIONS General laboratory skills and critical thinking. Organizational, time-management and record-keeping skills. Interpersonal and communication skills. Flexibility with changing objectives and priorities. Working knowledge of Microsoft Office including OneDrive, Teams, and OneNote. Ability to read, write and speak in English is required. Communicating in Spanish is a valuable skill at Helena. Travel by various means up to 10% of the time is required, including sitting in a vehicle for long periods of time. Valid U.S. driver's license is required to drive a company vehicle. Successful completion of a drug test and background check is required for all positions at Helena. WORK ENVIRONMENT & PHYSICAL ASPECTS OF THE JOB The work environment for this position is that of a typical office environment where the noise level is mostly quiet. This position requires you to use your hands for many different tasks and to talk, hear, walk, stand and sit. You may be occasionally required to lift or move up to 10 pounds. BENEFITS AT HELENA Health, Dental & Vision Insurance STARTS THE SAME DAY YOU DO! Earn up to $3,000 in Reward Dollars from Helena for your Health Savings Account (HSA). Helena's robust 401(k) Savings Plan offers you a 100% company-match up to 5% starting on your first day. As your years of service with Helena increase, so does our company-match - up to 10% based on your contribution amount. Three-year vesting on company match with 1,000 hours of service. Access your earned pay between paydays through Earned Wage Access (EWA) with DailyPay. Up to 15 days paid time-off plus 9 paid holidays. Free Term Life Insurance at 1x your annual base pay - paid for by Helena at no cost to you. Free Short & Long-Term Disability. Up to 80 hours of paid Parental Leave. Education Assistance. And much more! For more detailed information about our benefits, visit helenacareers.com/benefits. STAY CONNECTED TO THE HELENA POWERHOUSE! Follow us on social @HelenaCareers or visit us at helenacareers.com. Helena supports individuals with disabilities, and reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Helena is an equal opportunity employer.

Desired Experience: Formulating or compounding resins Hands on laboratory experience in SMC, BMC, or Pultrusion molding processes. Experience in formulation and compounding of unsaturated polyester and epoxy vinyl ester resins Graduate research in polymer science (synthesis, compounding, or materials science) Required Skills: Excellent knowledge in resin chemistry formulations and compounding Hands-on laboratory skills Knowledge of physical testing and mechanical properties Excellent organizational and project management skills Strong written and oral communication skills Interpersonal skills for customer and colleague collaboration Microsoft Office Additional Desired Skills and Characteristics: Proven track record in product development, ability to recite and quantify these successes Creativity, curiosity, mechanically inclined, problem solving, time management, ability to seek out and find new opportunities for composites, business acumen. Required Qualifications: M.S. in Polymer Science, Material Science, Chemistry, Chemical Engineering, Composites Engineering or related field. (Ph.D. candidates will be considered). Other: Minimal travel, up to 10% Applicants must be currently authorized to work in the US on a full-time basis. This position is not eligible for immigration sponsorship. : The Scientist, Structural Composite Molding Formulations at AOC will be based in Valparaiso, Indiana. The main responsibilities are product development of AOC products for composite applications that are using sheet molding compound, bulk molding compound and pultrusion. Examples of end uses are construction, automotive and infrastructure. The position is hands on with formulating, compounding and molding. The candidate should be mechanically inclined as well as have excellent chemical formulation knowledge, specifically with unsaturated polyester and epoxy vinyl ester chemistries. The individual will support the product leaders and the technical manager in design of experiments, formula development, preparing samples with hands on laboratory work, maintaining equipment, molding, and authoring technical reports. Organization and project management skills are important as well as business acumen. Salary is negotiable and commensurate with experience. Individuals with experience and skills far exceeding those in this job descriptions will be eligible for a senior material scientist role.

Market Range: 05 Hiring Range: $19.10/Hourly THIS IS A PART-TIME GRANT FUNDED POSITION FUNDED UNTIL XXX (20 HOURS PER WEEK) JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Technician 2 plans, implements, analyzes data needed for our large database studies, primarily working with software and datasets such as TriNetX, SEER-Medicare and other clinical datasets. This position assist with IRB and other regulatory requirements for the study. EDUCATION: Bachelor's Degree. (TRANSCRIPT REQUIRED) EXPERIENCE: OR Combination of college course work and work experience to equal four (4) years. KNOWLEDGE, SKILLS, ABILITIES: CITI training. Skill with SAS or R-programming. HIPAA training. Coordinates and prepares laboratory meetings with the Principal Investigator. Performs weekly updates on data cleaning, analysis, and planning. Performs regulatory checks. Writes scientific papers, submissions, and attends poster presentations. Performs data cleaning and reviews and assesses statistical methodology and data analysis. Assist with IRB and regulatory approvals. Assists in grant writing, manuscript preparation, and future analysis. Performs other duties as assigned.

The University of Alabama at Birmingham, Med - Infectious Diseases, is looking for a dedicated Researcher Associate to join their team to perform various support function in a research laboratory using appropriate procedures to generate and validate data of sufficient quality for project development, publication, and grant submissions. General Responsibilities As a Researcher Associate, this intermediate-level position will require you to independently conduct more complex studies and analyses, contributing to the advancement of research projects. With greater autonomy, you will design experiments, interpret data, and collaborate with senior researchers to develop and refine research protocols. Your role may also include mentoring junior staff and ensuring compliance with safety and regulatory standards. Depending on the research focus, this position may involve research collaborator contact, research animal contact, and/or specimens. Key Duties & Responsibilities * Perform various support functions in a research laboratory while also maintaining equipment, computer database and lab supplies. * Document daily laboratory activities and results. * Perform other duties as assigned. Hourly Range: $ 19.80- $ 32.15 Qualifications Bachelor's degree in a related field OR Associate's degree in a related field and two (2) years of related experience OR High School diploma or GED and four (4) years of related experience required. Work experience may NOT substitute for education requirement. Preferences * Two years of related lab experience preferred. * Ability to work as part of a team. UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

The Scientist performs and/or coordinates a wide range of laboratory research procedures and conducts a spectrum of complex support tasks and projects determined by the field and scope of the particular research study. Also, performs a variety of laboratory techniques independently and presents results. The Associate Scientist performs a variety of moderately complex research tasks determined by the field and scope of the particular research project/study. Also, performs tasks related to the research project independently, but within broad guidelines and subject to periodic review by supervisor or other research staff. At St. Jude Children's Research Hospital, talented faculty and staff work together and with colleagues worldwide to advance the research and treatment of pediatric cancer and other catastrophic diseases. We are seeking an outstanding, highly motivated, and creative Scientist to join Dr. Jonathan Yen's lab and the Therapeutic Genome Engineering (TGEn) group. You will be part of a multidisciplinary team of scientists and clinical researchers helping to advance genome editing strategies for treating sickle cell disease to a Phase 1 clinical trial. Our ongoing therapeutic pipeline is fueled by internal scientific discoveries directed from “bench-to-bedside” and academic collaborations. Come join TGEn to en GENEer concepts to cures! You will have the opportunity to work with a talented interdisciplinary team of scientists to develop a cellular therapy with the goal of treating patients here at St. Jude Children's Research Hospital and worldwide. The ideal candidate will have a strong combination of experience with genome editing and human hematopoietic stem cells (HSCs). You will also have the opportunity to learn about and support new, exciting projects, including the development and optimization of pre-clinical genome editing strategies to treat hemoglobinopathies and other hematological diseases, process development, and IND-enabling studies (Pharm/Tox). Job Responsibilities: Perform studies to develop genome editing strategies for human hematopoietic stem cells (HSC). Design and execute IND-enabling experiments to characterize the pharmacology of a genome-edited human hematopoietic stem cell product to treat sickle cell disease. Characterize the efficacy, safety, and potency of the HSC cellular drug product in in vitro and xenotransplantation assays. Multicolor flow cytometry and FACS to sort hematopoietic populations of relevance. Develop experimental methods including RT-PCR, dd PCR, next-generation sequencing, and single-cell sequencing. Perform NGS library preparation and analysis of editing outcomes, on-target and off-target. Evaluate scale-up and close-system processes to ensure reproducibility of the drug product. Conduct exploratory research on developing novel in-vitro and in-vivo delivery strategies. Interact and collaborate with multidisciplinary teams to advance the program. Establish tracking and trending analyses of process development and pilot runs. Draft documentation (protocols, batch records, reports) to standardize and transfer process to GMP facility. Maintains regular and predictable attendance. Performs other related duties as assigned to meet the goals of the department and institution. Minimum Education and/or Training: Bachelor's degree in a relevant scientific area is required. Master's or PhD degree in a relevant scientific area is highly preferred. Associate Scientist Minimum Experience: 7 + years of research experience is required 5 + years of research experience is required with a Master's degree 2 + years of research experience is required with a PHD Experience leading and supporting research experiments preferred Some experience leading lab and scientific project coordination, maintenance, and other research support activities preferred Experience in guiding and training other laboratory personnel preferred Proven performance in earlier role/comparable role Salary range: $65,520.00 - $114,400.00 Scientist Minimum Experience: Eight (8) years of relevant post-degree work experience is required with a Bachelor's degree. Six (6) years of relevant post-degree work experience is required with a Master's degree. Three (3) years of relevant post-degree work experience is required with a PhD. Experience leading and supporting research experiments preferred. Some experience leading lab and scientific project coordination, maintenance, and other research support activities preferred. Experience in guiding and training other laboratory personnel preferred. Proven performance in earlier role/comparable role. Salary range: $86,320.00 - $154,960.00 Welcome to Memphis This position is based in Memphis, TN; relocation assistance is available. Memphis is a family-friendly metropolitan area that more than a million residents call home. Memphis is recognized for its world-class music, food, and hospitality. Cost of living is one of our biggest attractions; in fact, Money listed Memphis as one of the least expensive cities in which to raise a child. Mild winters and beautiful green spaces make the city a magnet for outdoor enthusiasts - there are over 200 miles of bike-friendly lanes with more being added. Forbes recently named Memphis the 4th happiest city in which to work. Apply today! A cover letter is highly recommended. Interested applicants should submit a cover letter as part of the application process. Please address your cover letter to: Jonathan Yen, PhD Department of Hematology Mail Stop 355 St. Jude Children's Research Hospital 262 Danny Thomas Place Memphis, TN 38105-3678 Compensation In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $86,320 - $154,960 per year for the role of Associate Scientist or Scientist - Yen Lab/Therapeutic Genome Engineering (TGEn Group). Explore our exceptional benefits! St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Position: Senior Manufacturing Technician or Senior Manufacturing Process Scientist Location: Memphis, TN Duration: Fulltime Permanent Relocation: Relocation Package is Provided Our Client is looking for Senior Manufacturing Process Scientist- With protein purification etc. experience…..!!!!! Position will be responsible for overseeing and executing the process design and manufacturing of monoclonal antibodies, polyclonal antibodies and recombinant proteins products and services sold into IVD industry. The Senior Manufacturing Process Scientist will possess ‘hands-on' experience with various forms of chromatography (affinity, ion exchange, HIC, etc.), centrifugation, TFF/DF/UF, cell culture and fermentation. Experience with aseptic techniques particularly useful in the areas of eukaryotic cell culture, bacterial and yeast fermentation. The individual must be capable of executing and authoring Master Batch Records and Standard Operating Procedures in compliance with current Good Manufacturing Practices. This position will supervise Production Technicians. SUMMARY & RESPONSIBILITIES: • Perform bio separation of recombinant proteins, monoclonal/polyclonal antibodies. Bioseparation methods to include, but not limited to, preparative centrifugation, TFF filtration, and chromatographic methods (ion exchange, size exclusion, affinity, etc.). • Familiar with In vitro cell culture of monoclonal antibodies and fermentation of recombinant proteins. • Develop and perform various analytical protein methods for process monitoring and characterization of in-process and final product. The methods to include but not limited to SDS-PAGE, Western Blot, ELISA, UV-VIS, and Immunoassays methods. • Assess feasibility of contract manufacturing cell culture and purification opportunities, participate in development of proposal and costing estimates. • Author master batch records and SOPs for transferred/developed process in compliance with all current GMP regulations and company SOPs. • Train Production Technicians in upstream and downstream manufacturing processes. • Develop strategies to improving yields and reducing overall manufacturing costs. Investigate alternative materials or new process equipment to improve efficiency. • Write and execute validation protocols for new and existing manufacturing processes. • Assist with the writing of technical reports, customer proposals, and product release specifications Qualifications QUALIFICATIONS AND SKILLS NEEDED: • Ph.D. with 3+ years of industrial experience or MS with 6+ years of industrial experience in a GMP or GLP environment. • Extensive knowledge and hands on experience of protein purification and characterization. • Experience with virus like proteins and viruses a plus. A knowledge of AKTA Unicorn software and disposable systems a plus. • Hands on experience with in vitro cell culture and recombinant protein fermentation • Ability to independently apply bioseparation basic theory and scientific principles to conduct downstream process development for proteins. • Proven experience with process scale-up procedures. • Extensive knowledge and hands on experience with protein analytical methods including (SDS-PAGE, Western Blot, ELISA, BCA, UV-VIS, HPLC methods etc). • Concise and accurate oral and written reporting of technical including batch records, SOPs, validation protocols and customer proposals. • MUST BE US CITIZEN or GREEN CARD holder only. Requirements (Physical, Mental, Environmental Demands): • Ability to walk up and down several flights of stairs throughout the work day in a multi-location facility. • Must be able to concentrate, analyze and solve complex issues throughout the course of the work day. • Ability to work on a PC including repetitive use of a keyboard and mouse for long periods throughout the course of the work day. • Ability to sit for long periods of time, stoop, reach, bend throughout the course of the work day. • Must be able to lift up to 30lbs. multiple times daily. • Must be able to travel by air/car to other locations of MBI as needed. • May be required to work outside normal business hours including evenings and/or weekends to support business needs. Additional Information Regards Pooja Mishra Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Tel: 732 429 1636 (W) 732-549-2030 x 214 | (F) 732-549-5549 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Desired Experience: Formulating or compounding resins Hands on laboratory experience in SMC, BMC, or Pultrusion molding processes. Experience in formulation and compounding of unsaturated polyester and epoxy vinyl ester resins Graduate research in polymer science (synthesis, compounding, or materials science) Required Skills: Excellent knowledge in resin chemistry formulations and compounding Hands-on laboratory skills Knowledge of physical testing and mechanical properties Excellent organizational and project management skills Strong written and oral communication skills Interpersonal skills for customer and colleague collaboration Microsoft Office Additional Desired Skills and Characteristics: Proven track record in product development, ability to recite and quantify these successes Creativity, curiosity, mechanically inclined, problem solving, time management, ability to seek out and find new opportunities for composites, business acumen. Required Qualifications: M.S. in Polymer Science, Material Science, Chemistry, Chemical Engineering, Composites Engineering or related field. (Ph.D. candidates will be considered). Other: Minimal travel, up to 10% Applicants must be currently authorized to work in the US on a full-time basis. This position is not eligible for immigration sponsorship. : The Scientist, Structural Composite Molding Formulations at AOC will be based in Valparaiso, Indiana. The main responsibilities are product development of AOC products for composite applications that are using sheet molding compound, bulk molding compound and pultrusion. Examples of end uses are construction, automotive and infrastructure. The position is hands on with formulating, compounding and molding. The candidate should be mechanically inclined as well as have excellent chemical formulation knowledge, specifically with unsaturated polyester and epoxy vinyl ester chemistries. The individual will support the product leaders and the technical manager in design of experiments, formula development, preparing samples with hands on laboratory work, maintaining equipment, molding, and authoring technical reports. Organization and project management skills are important as well as business acumen. Salary is negotiable and commensurate with experience. Individuals with experience and skills far exceeding those in this job descriptions will be eligible for a senior material scientist role.

Market Range: 05 Hiring Salary: $19.10/Hourly FUNDED UNTIL 10/31/2027 JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the Principal Investigator, Research Technician 2 conducts experiments following the behaviors of mice. EDUCATION: Bachelor's Degree. (TRANSCRIPT REQUIRED) EXPERIENCE: OR a combination of college coursework and work experience to equal four (4) years. KNOWLEDGE, SKILLS, AND ABILITIES: Skill in database analysis. Knowledge of brain surgery, brain Ca2+ imaging in vivo, behavioral testing, brain histology, and computational/statistical analyses. Ability to work independently, self-motivated and detail oriented. Assists with mouse brain surgery, molecular/cellular biology, and Ca2+ imaging. Assists in behavioral testing. Performs data analysis with assistance. Assists with brain clearing and imaging. Orders and maintains lab materials and equipment. Maintains and handle mouse lines in the vivarium. Assists with genotyping for the mouse lines. Performs other related duties as assigned.

Category Laboratory Sciences & Support Department Developmental Neurobiology Shift Weekday Day Type Full Time Scheduled Weekly Hours 40 Req # JR6111 Job Description An Associate Scientist performs a variety of moderately complex research tasks determined by the field and scope of the particular research project/study. Also, performs tasks related to the research project independently, but within broad guidelines and subject to periodic review by supervisor or other research staff. An Associate Scientist position is available for a highly motivated scientist with a background in Circuits or Systems Neuroscience to coordinate the application of in vivo methodologies to assess neural function and animal behavior with multiple labs in the Developmental Neurobiology (DNB) department. This position is well-suited for an individual interested in transitioning from a postdoctoral position to a more stable, long-term position. The successful candidate will work directly with DNB labs to establish standard and innovative approaches for monitoring animal behavior in a wide variety of assays (motor, stress, cognitive, etc). It's expected that qualified candidates would have direct experience with several of the following methodologies: optogenetics, fiber photometry, in vivo calcium imaging, and/or machine-learning-based behavioral assessment. Additionally, it will be important for candidates to have familiarity with basic coding practices to coordinate data collection across multiple platforms (e.g, coordinating calcium imaging or optogenetic delivery with behavioral tracking). Job Responsibilities: * Perform behavior-related experiments in collaboration with DNB lab members for the establishment and advancement of current projects. * Implement and optimize algorithms for analyzing behavior data. * Build or implement existing scripts to temporally align data across multiple modalities. * Coordinate efforts with DNB researchers and established vendors (Med Associates, Inscopix, TDT Systems) to troubleshoot and optimize behavior-related data collection. * Contribute to publications and presentations of research findings * Maintains regular and predictable attendance * Work independently and collaboratively with DNB labs. * Provide guidance and training to less-experienced team members and may also train others outside the lab in relevant techniques. * Perform other duties as assigned to meet the goals and objectives of the department and the institution. * Maintain regular and predictable attendance. Preferred Qualifications: * PhD in neuroscience, biology, computational neuroscience, or related fields. * Demonstrated hands-on experience with neural circuit-based approaches. * Strong programming skills (Python preferred). * Experience analyzing time-series data, preferably from neuroimaging or behavioral studies. * Knowledge of statistical analysis. * Excellent communication skills and ability to work in a collaborative environment. Minimum Education and/or Training: * Bachelor's degree in a relevant scientific area Minimum Experience: * 7+ years of research experience is required * 5+ years of research experience is required with a Master's degree * 2+ years of research experience is required with a PHD * Experience leading and supporting research experiments preferred * Some experience leading lab and scientific project coordination, maintenance, and other research support activities preferred * Experience in guiding and training other laboratory personnel is preferred * Proven performance in earlier role/comparable role. Preference will be given to applicants who have a strong background in leveraging in vivo approaches to solve complex problems in behavioral neuroscience. The candidate will also benefit from an outstanding, highly collaborative work environment in which research labs have diverse interests in understanding the underlying mechanisms of neural circuit function related to neuromodulation, motor output, and psychiatric disease. The Department of Developmental Neurobiology houses specialized departmental shared resources, including an integrated support structure for in vivo and ex vivo neuroimaging, behavioral phenotyping, computational neuroscience, genetic engineering, and single-cell genomics. In addition, numerous institutional shared resources and core facilities support the laboratory by providing expertise and state-of-the-art technologies. Compensation In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $65,520 - $114,400 per year for the role of Associate Scientist - Circuits/Systems/Behavioral Neuroscience. Explore our exceptional benefits! St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Our client is a public and rapidly growing diagnostics company that is looking to expand their Quality team in Memphis TN. They are willing to assist with relocation. Relocation assistance is provided! Excellent benefits, competitive salary, and stock options. Job Description Under direct supervision, responsible for design, performance and interpretation of experiments in support of the company's product development. Responsibilities: Responsible for the design and conduct of experiments as defined by work streams in accordance with the company's Quality System and to regulatory standards Ensures that work is completed to agreed timelines, communicating delays or issues to supervisor in timely manner Prioritizes workload to insure key objectives are met on time May supervise the work of a junior member of staff Presents data at internal and external meetings Ensures that conclusions in written reports reflect the data presented and reports are of the highest quality When required, operate as a scientist in support of running Laboratories, ensuring that the Quality Management System, including ISO 9001:2008, ISO 13485:2003, CLIA and CAP, is adhered to at all times and in all aspects of the job Perform other duties in departments on an occasional basis to meet critical company objectives Follows all company safety policies & other safety precautions within work area Regular attendance and timeliness is essential Qualifications BS or MS Degree in life sciences, Higher preferred Experience with cell culture techniques imperative Hands-on experience with flow cytometry and PCR techniques Demonstrated understanding of the diagnostic and pharmaceutical industries Familiarity with Quality System concepts and requirements including GMP and ISO Working knowledge of ELISA and ELISPOT a distinct advantage Expert at analyzing data Must be proficient in MS Office Additional InformationAll your information will be kept confidential according to EEO guidelines.

As a Researcher Technician, this entry-level position will play a pivotal role in supporting team operations within a dynamic research environment. Under the guidance of managers, team leads, or senior technicians, you will conduct routine tests/measures and assist in various research endeavors. Your responsibilities will include aiding investigators or senior researchers in conducting studies and procedures encompassing tasks such as data collection, solution preparation, and equipment setup and maintenance. Depending on the research focus, this position may involve research collaborator contact, research animal contact, and/or specimens. Position will work in scientific research lab conducting experiments, ordering supplies, and troubleshooting equipment in the lab. Duties and Responsibilities: * Conduct experiments in accordance with study protocols * Order Supplies * Troubleshoot equipment * Prepare equipment for laboratory experiments * Perform other duties as assigned Salary range: $31,200 - $50,750 High School or GED required. Previous research experience or coursework preferred. UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

Desired Experience: Formulating or compounding resins Hands on laboratory experience in SMC, BMC, or Pultrusion molding processes. Experience in formulation and compounding of unsaturated polyester and epoxy vinyl ester resins Graduate research in polymer science (synthesis, compounding, or materials science) Required Skills: Excellent knowledge in resin chemistry formulations and compounding Hands-on laboratory skills Knowledge of physical testing and mechanical properties Excellent organizational and project management skills Strong written and oral communication skills Interpersonal skills for customer and colleague collaboration Microsoft Office Additional Desired Skills and Characteristics: Proven track record in product development, ability to recite and quantify these successes Creativity, curiosity, mechanically inclined, problem solving, time management, ability to seek out and find new opportunities for composites, business acumen. Required Qualifications: M.S. in Polymer Science, Material Science, Chemistry, Chemical Engineering, Composites Engineering or related field. (Ph.D. candidates will be considered). Other: Minimal travel, up to 10% Applicants must be currently authorized to work in the US on a full-time basis. This position is not eligible for immigration sponsorship. : The Scientist, Structural Composite Molding Formulations at AOC will be based in Valparaiso, Indiana. The main responsibilities are product development of AOC products for composite applications that are using sheet molding compound, bulk molding compound and pultrusion. Examples of end uses are construction, automotive and infrastructure. The position is hands on with formulating, compounding and molding. The candidate should be mechanically inclined as well as have excellent chemical formulation knowledge, specifically with unsaturated polyester and epoxy vinyl ester chemistries. The individual will support the product leaders and the technical manager in design of experiments, formula development, preparing samples with hands on laboratory work, maintaining equipment, molding, and authoring technical reports. Organization and project management skills are important as well as business acumen. Salary is negotiable and commensurate with experience. Individuals with experience and skills far exceeding those in this job descriptions will be eligible for a senior material scientist role.

Market Range: 05 Hiring Salary: $19.10/Hourly FUNDED UNTIL JANUARY 1, 2028 JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the Principal Investigator, the Research Technician 2 performs rodent handling and in vitro cell-based assays. MINIMUM REQUIREMENTS: EDUCATION: Bachelor's Degree in Biology, Psychology, Mathematics, Computer Science, or a related field. (TRANSCRIPT REQUIRED) EXPERIENCE: OR a combination of college coursework and work experience to equal four (4) years. KNOWLEDGE, SKILLS, AND ABILITIES: Meticulous record-keeping skills with attention to detail. Basic computer skills. Excellent communication and presentation skills. Ability to work as part of a team and follow directions. Ability to plan and complete experiments in a timely manner and around the schedule of important collaborators and institutional cores. WORK SCHEDULE: This position may occasionally be required to work weekends and evenings. May require occasional overnight travel. Performs in vitro cell-based assays in primary neuronal and astrocyte cultures. Assists with nucleic acid extractions, protein extractions, and other basic molecular biology as needed. Supports all aspects of rodent studies including colony maintenance, estrus cycle monitoring, timed matings, embryo collection, blood collection, tissue collections, perfusions, and injection. Performs behavioral phenotyping assays. Performs stereotaxic injections to deliver viral vectors to select rodent brain regions. Assists in the publication and presentation of data papers at internal and external meetings. Prepares weekly reports for lab meetings. Performs other related duties as assigned.

Category Laboratory Sciences & Support Department Cell and Molecular Biology Shift Weekday Day Type Full Time Scheduled Weekly Hours 40 Req # JR6128 Job Description We are seeking a highly motivated and talented associate scientist to join our team and lead cutting-edge research investigating the therapeutic potential of intrinsically disordered regions. The project will leverage pooled lentiviral screening pipelines of peptide inhibitors to systematically perturb key molecular interactions. This is an exciting opportunity to apply innovative high-throughput screening technologies to reveal new regulatory mechanisms and therapeutic targets. The successful candidates will play a central role in developing and implementing advanced lentiviral-based screening platforms across diverse biological systems, working at the interface of molecular biology, genomics, and translational discovery. The World's Brightest Minds Always Innovate At St. Jude Children's Research Hospital, we know what can be achieved when the brightest scientific minds face the fewest barriers. That's why we provide world-class facilities. State-of-the-art technologies. Extraordinary support. And a collaborative, bench-to-bedside environment where you can see, firsthand, how your science translates into survival for the children we serve. Quite simply, at St. Jude, we encourage you to dream big and stop at nothing when it comes to finding cures and saving children. Key Responsibilities: * Design, optimize, and execute pooled lentiviral screening workflows for large-scale peptide inhibitor characterization * Collaborate closely with bioinformaticians and project investigators to ensure robust experimental design, data acquisition, and analysis. * Support the development of innovative experimental strategies to expand and enhance existing screening capabilities. * Contribute to collaborative research outputs, including publications and conference presentations. Ideal Candidate: * PhD (or equivalent experience) in Molecular Biology, Cell Biology, Genetics, or a closely related field. * Demonstrated expertise in the design, production, and application of lentiviral vectors for genetic manipulation and screening. * Proven track record in developing, implementing, or applying high-throughput genetic perturbation or functional screening approaches. * Excellent organisational, communication, and record-keeping skills. * Strong problem-solving ability and capacity to work independently as well as collaboratively. Desirable Attributes: * Extensive expertise in the design, production, and application of lentiviral libraries for large-scale screening. * Familiarity with large-scale data generation and interpretation in screening contexts. * Proven expertise in the design and execution of assays to characterise protein-protein interactions. * Evidence of contributions to collaborative research initiatives or consortia. About the Research Environment: The Davey lab has recently joined the Department of Cell and Molecular Biology to launch a research program applying high-throughput screening approaches to uncover the therapeutic potential of intrinsically disordered regions. The post-holder will work within a collaborative, supportive team and benefit from world-class core facilities and excellent opportunities for professional development. What problem are we tackling? Target discovery is a critical foundation of drug development, underpinning efforts to overcome the persistent challenges of drug resistance, emerging pathogens, and complex diseases that lack effective therapies. By uncovering novel proteins and molecular pathways driving disease progression, we can enable the rational design of more selective interventions that reduce off-target effects and improve patient outcomes. The development of tool molecules, coupled with detailed characterization of their inhibitory mechanisms, provides a direct bridge between phenotypic observations and small-molecule drug design, accelerating the translation of basic discoveries into clinically actionable therapies. What is our approach? Short Linear Motifs (SLiMs) are compact functional modules embedded within the intrinsically disordered regions of proteins. They mediate a wide range of regulatory processes, including the assembly of dynamic complexes, recruitment of modifying enzymes, control of protein stability, and specification of subcellular localisation. Despite their central role in cellular regulation, SLiM-binding pockets remain a largely untapped class of therapeutic targets. By applying large scale base-editing and peptide inhibitor studies the project will address three key questions: (i) How essential are SLiM-mediated interactions for cellular fitness? (ii) Does SLiM essentiality differ between healthy and diseased cells? (iii) Can these interactions be selectively targeted for therapeutic intervention? Minimum Education and/or Training: * Bachelor's degree in a relevant scientific area Minimum Experience: * 7 + years of research experience is required with a Bachelor's degree. * 5 + years of research experience is required with a Master's degree. * 2 + years of research experience is required with a PhD. Better at Work. Better at Life. When you work at St. Jude, you'll join a highly collaborative work culture that inspires you every day to be your best. With opportunities for learning and growth, you can shape a career path that is right for you while also enjoying all the benefits and stability of working for a world-class institution. This includes work-life balance with generous paid time-off and on-campus conveniences that make life a little easier. Join us and you'll quickly see why St. Jude is consistently ranked by our employees on Glassdoor as a "Best Place to Work." Benefits Your health and well-being are important to us. That's why St. Jude Children's Research Hospital provides employees with high-quality benefits choices. We are committed to ensuring our benefits are competitive and affordable. St. Jude continues to cover medical premiums for employees and offers low additional costs for dependents. View all the benefits offered including Medical & Prescription Drug Plans, Dental Plan, Vision Plan, Financial Security, Retirement Plan, Living Well - Employee Wellness Program, Time Off Programs, Educational Benefits, Family Friendly Benefits, and Benefits Unique to St. Jude. Have More in Memphis Get the best of big-city amenities mixed with all the charm of a small-town feel when you live in Memphis. From our world-renowned music scene to our eclectic mix of food and people. Memphis is a place our employees are proud to call home. Our region enjoys a cost of living more than 20% lower than the national average and our state places no personal income tax on wages. Plus, Memphians spend five hours less per year in their daily commute compared to the national average. Learn how you can "Have More in Memphis." Compensation In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $65,520 - $114,400 per year for the role of Associate Scientist (Pooled Lentiviral Base Editing Screening). Explore our exceptional benefits! St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Our client is a public and rapidly growing diagnostics company that is looking to expand their Quality team in Memphis TN. They are willing to assist with relocation. This position will have no direct reports. Overview: This position is responsible for carrying out T-SPOT assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the running of the Quality Management System and general administration of documentation for the QMS. This will include the following: Responsibilities: Overall responsibilities: 1. Maintenance of reference material, including cell culture and stock validation 2. QC of raw materials, incoming goods and any product manufactured by Oxford Immunotec 3. QC of manufactured products and assembled kits 4. Validation of procedures, equipment and software 5. Planning and conducting of stability testing procedures 6. Performing other laboratory testing as required 7. Maintaining the equipment databases to ensure all equipment is calibrated, maintained and serviced as required 8. Assisting with the control of Quality Management system documentation 9. Assisting with the preparation of further documentation for the Quality Management system 10. Assisting with the monitoring of compliance with the QMS and with tracking systems associated with CLIA, CAP, State requirements, ISO 13485:2012, ISO 9001:2008 and ISO 17025:2005 and the QSR 11. Assist the Quality Manager to ensure the continuing effectiveness of the QMS 12. Assist during internal and external audits 13. Conduct laboratory spot check audits 14. Assist with the QA review of documentation including non-conformances, CAPAs and complaints 15. Perform miscellaneous duties as necessary and requested by the Quality Manager Specific deliverables for the role are: 1. Contributing towards the maintenance of the quality of the Company's products in fulfillment of the Company goals 2. Control and conduct of product stability testing to support expiry dates and shipping claims 3. Monitoring of product conformity through archive kit testing 4. Assisting with ensuring compliance in the manufacturing process and documentation 5. Ensure that areas of responsibility do not contribute to any major non-conformance during external audits for GMP, ISO 13485:2003, ISO 17025:2005 and ISO 9001:2008 6. Regular communication with QA/QC team members and other functional groups to provide QC and validation support for both Process and Design controls 7. Working to Oxford Immunotec's Company Values at all times. 8. Follows all company safety policies & other safety precautions within work area 9. Regular attendance and timeliness is essential Qualifications QUALIFICATIONS: • Bachelor's degree, or college education and equivalent experience • 5+ years Quality experience, preferably in laboratory or medical device environmen ***Must have cell culture experience*** • Good working knowledge of MS Office • Experienced in working to GLP and Quality Management principles • Strong attention to detail and Quality commitment • High standards of mathematics and writing ability • Conscientious, thrives in high pressure work, and demonstrates strong initiative PHYSICAL DEMANDS: The physical demands described within the Position Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Minimal travel required including international travel. Job requires employee to walk considerable distances in the facility during the course of his or her work. Additional InformationAll your information will be kept confidential according to EEO guidelines.

We are seeking a highly motivated and talented associate scientist to join our team and lead cutting-edge research investigating the therapeutic potential of intrinsically disordered regions. The project will leverage pooled lentiviral screening pipelines of peptide inhibitors to systematically perturb key molecular interactions. This is an exciting opportunity to apply innovative high-throughput screening technologies to reveal new regulatory mechanisms and therapeutic targets. The successful candidates will play a central role in developing and implementing advanced lentiviral-based screening platforms across diverse biological systems, working at the interface of molecular biology, genomics, and translational discovery. The World's Brightest Minds Always Innovate At St. Jude Children's Research Hospital, we know what can be achieved when the brightest scientific minds face the fewest barriers. That's why we provide world-class facilities. State-of-the-art technologies. Extraordinary support. And a collaborative, bench-to-bedside environment where you can see, firsthand, how your science translates into survival for the children we serve. Quite simply, at St. Jude, we encourage you to dream big and stop at nothing when it comes to finding cures and saving children. Key Responsibilities: Design, optimize, and execute pooled lentiviral screening workflows for large-scale peptide inhibitor characterization Collaborate closely with bioinformaticians and project investigators to ensure robust experimental design, data acquisition, and analysis. Support the development of innovative experimental strategies to expand and enhance existing screening capabilities. Contribute to collaborative research outputs, including publications and conference presentations. Ideal Candidate: PhD (or equivalent experience) in Molecular Biology, Cell Biology, Genetics, or a closely related field. Demonstrated expertise in the design, production, and application of lentiviral vectors for genetic manipulation and screening. Proven track record in developing, implementing, or applying high-throughput genetic perturbation or functional screening approaches. Excellent organisational, communication, and record-keeping skills. Strong problem-solving ability and capacity to work independently as well as collaboratively. Desirable Attributes: Extensive expertise in the design, production, and application of lentiviral libraries for large-scale screening. Familiarity with large-scale data generation and interpretation in screening contexts. Proven expertise in the design and execution of assays to characterise protein-protein interactions. Evidence of contributions to collaborative research initiatives or consortia. About the Research Environment: The Davey lab has recently joined the Department of Cell and Molecular Biology to launch a research program applying high-throughput screening approaches to uncover the therapeutic potential of intrinsically disordered regions. The post-holder will work within a collaborative, supportive team and benefit from world-class core facilities and excellent opportunities for professional development. What problem are we tackling? Target discovery is a critical foundation of drug development, underpinning efforts to overcome the persistent challenges of drug resistance, emerging pathogens, and complex diseases that lack effective therapies. By uncovering novel proteins and molecular pathways driving disease progression, we can enable the rational design of more selective interventions that reduce off-target effects and improve patient outcomes. The development of tool molecules, coupled with detailed characterization of their inhibitory mechanisms, provides a direct bridge between phenotypic observations and small-molecule drug design, accelerating the translation of basic discoveries into clinically actionable therapies. What is our approach? Short Linear Motifs (SLiMs) are compact functional modules embedded within the intrinsically disordered regions of proteins. They mediate a wide range of regulatory processes, including the assembly of dynamic complexes, recruitment of modifying enzymes, control of protein stability, and specification of subcellular localisation. Despite their central role in cellular regulation, SLiM-binding pockets remain a largely untapped class of therapeutic targets. By applying large scale base-editing and peptide inhibitor studies the project will address three key questions: (i) How essential are SLiM-mediated interactions for cellular fitness? (ii) Does SLiM essentiality differ between healthy and diseased cells? (iii) Can these interactions be selectively targeted for therapeutic intervention? Minimum Education and/or Training: Bachelor's degree in a relevant scientific area Minimum Experience: 7 + years of research experience is required with a Bachelor's degree. 5 + years of research experience is required with a Master's degree. 2 + years of research experience is required with a PhD. Better at Work. Better at Life. When you work at St. Jude, you'll join a highly collaborative work culture that inspires you every day to be your best. With opportunities for learning and growth, you can shape a career path that is right for you while also enjoying all the benefits and stability of working for a world-class institution. This includes work-life balance with generous paid time-off and on-campus conveniences that make life a little easier. Join us and you'll quickly see why St. Jude is consistently ranked by our employees on Glassdoor as a “Best Place to Work.” Benefits Your health and well-being are important to us. That's why St. Jude Children's Research Hospital provides employees with high-quality benefits choices. We are committed to ensuring our benefits are competitive and affordable. St. Jude continues to cover medical premiums for employees and offers low additional costs for dependents. View all the benefits offered including Medical & Prescription Drug Plans, Dental Plan, Vision Plan, Financial Security, Retirement Plan, Living Well - Employee Wellness Program, Time Off Programs, Educational Benefits, Family Friendly Benefits, and Benefits Unique to St. Jude. Have More in Memphis Get the best of big-city amenities mixed with all the charm of a small-town feel when you live in Memphis. From our world-renowned music scene to our eclectic mix of food and people. Memphis is a place our employees are proud to call home. Our region enjoys a cost of living more than 20% lower than the national average and our state places no personal income tax on wages. Plus, Memphians spend five hours less per year in their daily commute compared to the national average. Learn how you can “Have More in Memphis.” Compensation In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $65,520 - $114,400 per year for the role of Associate Scientist (Pooled Lentiviral Base Editing Screening). Explore our exceptional benefits! St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.